Canonical Allele Identifier: CA468400801
Gene: GATA3 HGNC NCBI

Linked Data

dbSNP Id: rs1239082325
gnomAD v4: 10-8058570-C-A
MyVariant Identifiers: chr10:g.8100533C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8058570C>A , CM000672.2:g.8058570C>A GRCh38
NC_000010.10:g.8100533C>A , CM000672.1:g.8100533C>A GRCh37
NC_000010.9:g.8140539C>A NCBI36
NG_015859.1:g.8867C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000346208.4:c.507C>A ENSP00000341619.3:p.Thr169=
ENST00000379328.9:c.507C>A MANE Select ENSP00000368632.3:p.Thr169=
ENST00000346208.3:c.507C>A ENSP00000341619.3:p.Thr169=
ENST00000379328.7:c.507C>A ENSP00000368632.3:p.Thr169=
ENST00000461472.1:n.172C>A
NM_001002295.1:c.507C>A NP_001002295.1:p.Thr169=
NM_002051.2:c.507C>A NP_002042.1:p.Thr169=
XM_005252442.2:c.507C>A XP_005252499.1:p.Thr169=
XM_005252443.3:c.507C>A XP_005252500.1:p.Thr169=
XM_005252443.5:c.507C>A XP_005252500.1:p.Thr169=
NM_001002295.2:c.507C>A MANE Select NP_001002295.1:p.Thr169=
NM_002051.3:c.507C>A NP_002042.1:p.Thr169=